首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   862篇
  免费   65篇
  国内免费   10篇
  2023年   14篇
  2022年   11篇
  2021年   18篇
  2020年   13篇
  2019年   12篇
  2018年   14篇
  2017年   13篇
  2016年   18篇
  2015年   20篇
  2014年   28篇
  2013年   31篇
  2012年   25篇
  2011年   15篇
  2010年   16篇
  2009年   20篇
  2008年   22篇
  2007年   30篇
  2006年   20篇
  2005年   15篇
  2004年   15篇
  2003年   8篇
  2002年   13篇
  2001年   9篇
  2000年   24篇
  1999年   21篇
  1998年   27篇
  1997年   19篇
  1996年   24篇
  1995年   37篇
  1994年   26篇
  1993年   16篇
  1992年   29篇
  1991年   29篇
  1990年   23篇
  1989年   17篇
  1988年   19篇
  1987年   37篇
  1986年   16篇
  1985年   15篇
  1984年   18篇
  1983年   11篇
  1982年   26篇
  1981年   17篇
  1980年   14篇
  1978年   11篇
  1977年   6篇
  1976年   9篇
  1972年   7篇
  1971年   10篇
  1970年   9篇
排序方式: 共有937条查询结果,搜索用时 16 毫秒
81.
Clustering or overexpression of the transmembrane form of the extracellular matrix proteoglycan agrin in neurons results in the formation of numerous highly motile filopodia-like processes extending from axons and dendrites. Here we show that similar processes can be induced by overexpression of transmembrane-agrin in several non-neuronal cell lines. Mapping of the process-inducing activity in neurons and non-neuronal cells demonstrates that the cytoplasmic part of transmembrane agrin is dispensable and that the extracellular region is necessary for process formation. Site-directed mutagenesis reveals an essential role for the loop between β-sheets 3 and 4 within the Kazal subdomain of the seventh follistatin-like domain of TM-agrin. An aspartic acid residue within this loop is critical for process formation. The seventh follistatin-like domain could be functionally replaced by the first and sixth but not by the eighth follistatin-like domain, demonstrating a functional redundancy among some follistatin-like domains of agrin. Moreover, a critical distance of the seventh follistatin-like domain to the plasma membrane appears to be required for process formation. These results demonstrate that different regions within the agrin protein are responsible for synapse formation at the neuromuscular junction and for process formation in central nervous system neurons and suggest a role for agrin''s follistatin-like domains in the developing central nervous system.  相似文献   
82.
目的:探讨加味星蒌承气汤对急性缺血性脑卒中患者神经功能及血脂、血液流变学的影响。方法:选取2017年8月~2019年6月期间我院收治的急性缺血性脑卒中患者96例,将入选患者根据随机数字表法分为对照组(n=48)和研究组(n=48),对照组患者予以常规西医治疗,研究组患者在对照组基础上联合加味星蒌承气汤治疗,对比两组患者疗效、神经功能及血脂、血液流变学情况,记录两组患者治疗期间不良反应情况。结果:研究组治疗8 d后的临床总有效率为91.67%(44/48),显著高于对照组患者的72.92%(35/48)(P0.05)。两组治疗8 d后加拿大神经功能评分量表(CNS)、美国国立卫生研究所卒中量表(NIHSS)评分均下降(P0.05),且研究组低于对照组(P0.05)。两组治疗8 d后总胆固醇(TC)、低密度脂蛋白胆固醇(LDL-C)、甘油三酯(TG)、全血黏度高切、全血黏度低切、血浆黏度、纤维蛋白原均下降(P0.05),且研究组低于对照组(P0.05);高密度脂蛋白胆固醇(HDL-C)升高(P0.05),且研究组高于对照组(P0.05)。两组不良反应发生率比较无明显差异(P0.05)。结论:急性缺血性脑卒中患者采用加味星蒌承气汤治疗,疗效显著,可有效改善患者神经功能及血脂、血液流变学,且安全性较好。  相似文献   
83.
摘要 目的:探讨入院时血清钙水平与高血压性脑出血血肿体积、神经功能及预后的关系。方法:选择2018年9月-2020年4月我院收治的高血压性脑出血患者102例,根据患者入院时血清钙水平将其分为低血钙组(血清钙<2.1 mmol/L, n=34)、正常血钙组(2.1 mol/L≤血清钙≤2.7 mmol/L, n=39)和高血钙组(血清钙>2.7 mmol/L, n=29),比较各组性别、血肿体积、入院美国国立卫生研究院卒中量表(NIHSS)评分等临床资料。所有患者随访1年,观察患者格拉斯哥预后量表(GOS)评分,根据患者预后情况将患者分为预后良好组(n=84)和预后不良组(n=18),比较两组血清钙、血肿体积、入院NIHSS评分、GOS评分。应用受试者工作特征(ROC)曲线分析血清钙水平对患者预后的预测价值。结果:三组血肿体积、入院NIHSS评分、GOS评分、1年病死率、1年再出血率、总预后不良率比较有统计学差异(P<0.05)。预后不良组血清钙水平、GOS评分显著低于预后良好组,血肿体积、入院NIHSS评分显著高于预后良好组(P<0.05)。Pearson相关性分析显示:高血压性脑出血患者入院时血清钙水平与脑出血血肿体积、入院NIHSS评分呈负相关,与GOS评分呈正相关(P<0.05)。ROC曲线分析显示入院时血清钙预测高血压脑出血不良预后的曲线下面积为0.129(95%CI:0.073~0.179)。结论:高血压性脑出血患者入院时血清钙水平与血肿体积、神经功能及预后存在一定关联,且入院时血清钙对高血压性脑出血不良预后具有一定预测价值。  相似文献   
84.
Bacopa monnieri (Linn.) Wettst. commonly known as waterhyssop, Brahmi plant, traditionally used for memory enhancement, nerve tonic, epilepsy, central nervous system (CNS), antidepressant, anxiety, blood pressure and antioxidant activities. Due to pharmaceutical demands its lost natural habitat. At this juncture we describe a resourceful protocol for micropropagation of water hyssop plant. Surface sterilized leaf and nodal explants were inoculated on basal MS semi-solid medium added with PGRs; auxins, cytokinins. Highest calli formation from leaf explants was obtained on NAA (2.5 mg−1) and showed (94.22%) accompanied via 2,4-D showed (2.5 mg−1; 82.43%), maximum calli formation in nodal explants was obtained on 2,4-D showed (2.5 mg−1; 71.14%) followed by NAA (2.5 mg−1) showed (62.15%), in internodes explants uppermost calli formation was obtained from 2,4-D showed (2.5 mg−1; 65.21%) followed by NAA (2.5 mg−1) showed (52.14%). The maximum somatic embryogenic callus, calli induction and formation (84%) was observed on 2,4-D + KIN (2.0 + 1.5 mg−1) amended solid medium. Uppermost shoot formation was observed in combination of IAA + BAP (1.0 + 1.0 mg−1) showed (78.54%) shoot formation followed by IBA (2.0 mg−1) alone showed (75.37%). The maximum shoot elongation was noticed from NAA + BAP (3.0 + 3.0 mg−1) with 21.21 cm followed by NAA (2.0 mg−1) showed (15.22 cm) although, chief root formation was obtained from IBA (2.0 mg−1) with 83.75% root formation along higher number of roots (47.43%) per shoot. Followed by IAA (2.0 mg−1) showed root induction (73.43%) and no of roots (38.54%) per shoot. In hardening under pot condition plants survivability (100%) was observed under glass house conditions, the present in vitro PTC techniques is extremely significant to gratifying its natural conservation.  相似文献   
85.
秦明杰  刘一浓  牟颖  卢映蓉  吴飞 《生物磁学》2013,(24):4624-4626
目的:使用乳液法制备含有神经生长因子(NGF)的电纺纤维,研究其外观形貌和机械强度等物理性能,以及制备过程中NGF活性的变化,纤维中NGF的担载量和纤维体外释放动力学,评价其能否成为理想的神经修复材料,为进一步将NGF电纺纤维应用于周围神经修复奠定基础。方法:将NGF水溶液分散于PLLA溶液,通过W/O乳液法制备静电纺丝缓释纤维,对纤维的外观形貌等物理性能等进行表征,使用Elisa方法测定制备过程中NGF活性的保持以及体外释放动力学。结果:NGF电纺纤维具备类似细胞外基质(ECM)的良好外观形貌和一定的机械强度,其中NGF活性保持19.58%士6.05%,体外有效释放11天。结论:本文制备的乳液法NGF电纺纤维具备良好的物理性能,能够持续缓释有效剂量的NGF,适合作为神经修复材料进行进一步研究。  相似文献   
86.
We have previously reported that NADPH oxidase 2 (Nox2) is up-regulated in spinal cord microglia after spinal nerve injury, demonstrating that it is critical for microglia activation and subsequent pain hypersensitivity. However, the mechanisms and molecules involved in Nox2 induction have not been elucidated. Previous studies have shown that Toll-like receptors (TLRs) are involved in nerve injury-induced spinal cord microglia activation. In this study, we investigated the role of TLR in Nox2 expression in spinal cord microglia after peripheral nerve injury. Studies using TLR knock-out mice have shown that nerve injury-induced microglial Nox2 up-regulation is abrogated in TLR2 but not in TLR3 or -4 knock-out mice. Intrathecal injection of lipoteichoic acid, a TLR2 agonist, induced Nox2 expression in spinal cord microglia both at the mRNA and protein levels. Similarly, lipoteichoic acid stimulation induced Nox2 expression and reactive oxygen species production in primary spinal cord glial cells in vitro. Studies on intracellular signaling pathways indicate that NF-κB and p38 MAP kinase activation is required for TLR2-induced Nox2 expression in glial cells. Conclusively, our data show that TLR2 mediates nerve injury-induced Nox2 gene expression in spinal cord microglia via NF-κB and p38 activation and thereby may contribute to spinal cord microglia activation.  相似文献   
87.
Changes in bone remodeling induced by pharmacological and genetic manipulation of β-adrenergic receptor (βAR) signaling in osteoblasts support a role of sympathetic nerves in the regulation of bone remodeling. However, the contribution of endogenous sympathetic outflow and nerve-derived norepinephrine (NE) to bone remodeling under pathophysiological conditions remains unclear. We show here that differentiated osteoblasts, like neurons, express the norepinephrine transporter (NET), exhibit specific NE uptake activity via NET and can catabolize, but not generate, NE. Pharmacological blockade of NE transport by reboxetine induced bone loss in WT mice. Similarly, lack of NE reuptake in norepinephrine transporter (Net)-deficient mice led to reduced bone formation and increased bone resorption, resulting in suboptimal peak bone mass and mechanical properties associated with low sympathetic outflow and high plasma NE levels. Last, daily sympathetic activation induced by mild chronic stress was unable to induce bone loss, unless NET activity was blocked. These findings indicate that the control of endogenous NE release and reuptake by presynaptic neurons and osteoblasts is an important component of the complex homeostatic machinery by which the sympathetic nervous system controls bone remodeling. These findings also suggest that drugs antagonizing NET activity, used for the treatment of hyperactivity disorders, may have deleterious effects on bone accrual.  相似文献   
88.
目的探讨补阳还五汤口服加药浴对坐骨神经传导速度的影响。方法60只SD大鼠暴露左侧坐骨神经。对照组只钳夹;实验组钳夹并加用补阳还五汤口服及药浴治疗。观察钳夹前和钳夹切除后大鼠坐骨神经传导速度(SNCV)。结果于2、4、6周分别测对照组、实验组的坐骨神经传导速度(SNCV)。各时间段实验组坐骨神经传导速度恢复快于对照组,P〈0.01。结论补阳还五汤口服加药浴对坐骨神经传导速度有明显的促进作用。  相似文献   
89.
Alterations in corneal innervations result in impaired corneal sensation, severe dry eye and damage to the epithelium that may in turn lead to corneal ulcers, melting and perforation. These alterations can occur after refractive surgery. We have discovered that pigment epithelium-derived factor (PEDF) plus docosahexaenoic acid (DHA or the docosanoid bioactive neuroprotectin D1 (NPD1)) induces nerve regeneration after corneal surgery that damages the stromal nerves. We found that PEDF is released from corneal epithelial cells after injury, and when DHA is provided to the cells it stimulates the biosynthesis of NPD1 by an autocrine mechanism. The combination of PEDF plus DHA also decreased the production of leukotriene B4 (LTB4), a neutrophil chemotactic factor, thereby decreasing the inflammation induced after corneal damage. These studies suggest that PEDF plus DHA and its derivative NPD1 hold promise as a future treatment to restore a healthy cornea after nerve damage.  相似文献   
90.
目的:观察分析单唾液酸四己糖神经节苷脂钠治疗急性期脑出血的临床疗效,总结其临床用药经验。方法:选取我院2010年7月至2012年7月急性期脑出血的患者86例,按照数字表随机抽取法分成2组,对照组43例使用常规治疗,观察组43例在常规治疗基础上,加用单唾液酸四己糖神经节苷脂钠治疗,观察对比两组的临床治疗效果。结果:观察组治疗后总有效率为93.0%(40/43)对照组治疗后总有效率为76.8%(33/43),两组治疗效果对比差异明显(P〈0.05),具有统计学意义。结论:单唾液酸四己糖神经节苷脂钠治疗急性期脑出血的临床疗效显著,优于常规治疗,可有效保护神经功能不受损。  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号